Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/101615
Type: Artigo de periódico
Title: A 1h Nmr And Molecular Modelling Investigation Of Diastereotopic Methylene Hydrogen Atoms
Author: Tormena C.F.
Freitas M.P.
Rittner R.
Abraham R.J.
Abstract: The 1H NMR spectra of methyl 3-bromo-2-methylpropionate (1a) and the corresponding chloro compound (2a) show no long-range coupling between the methyl and methylene protons. In contrast, in the analogous dihalocompounds, methyl 2,3-dibromo-2-methylpropionate (1b) and methyl 2,3-dichloro-2-methylpropionate (2b), one of the methylene protons exhibits a large 4JHH coupling (0.8 Hz) to the methyl group, but the other proton shows no observable splitting. This can be explained quantitatively by calculations of the conformational preferences in these compounds combined with the known orientation dependence of the 4JHH couplings. One conformer predominates in the dihalo compounds 1b and 2b, and this is responsible for the 4JHH coupling. In 1a and 2a all three conformers are populated and the 4JHH couplings average to zero. The technique is a potentially general method of unambiguously assigning diastereotopic methylene protons. Copyright © 2002 John Wiley & Sons, Ltd.
Editor: 
Rights: fechado
Identifier DOI: 10.1002/mrc.1011
Address: http://www.scopus.com/inward/record.url?eid=2-s2.0-0142087912&partnerID=40&md5=953e2b4a9b58b1adef1d8afbecee1fea
Date Issue: 2002
Appears in Collections:Unicamp - Artigos e Outros Documentos

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